NDC 55111-194 - Fexofenadine Hydrochloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
55111-194
Manufacturer
Rebel Distributors Corp
Effective date
2011-01-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Fexofenadine Hydrochloride - Rebel Distributors CorpRebel Distributors Corp2011-01-27HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55111-194-01EA - Each55111-194b62c337a-6116-4b3d-8a54-72ba74eaa50312012-07-24
55111-194-05EA - Each55111-194bfcb051a-33e6-41fb-8d55-418c0baf9b2212013-02-11
55111-194-90EA - Each55111-194f1b495d7-0255-48f3-ad90-64f79f3bfadb12012-07-24

DailyMed Socrata Ingredients#